Total synthesis of pyrrolo[2,3-c]quinoline alkaloid: trigonoine B

The first total synthesis of the pyrrolo[2,3-c]quinoline alkaloid trigonoine B (1) was accomplished via a six-step sequence involving the construction of an N-substituted 4-aminopyrrolo[2,3-c]quinoline framework via electrocyclization of 2-(pyrrol-3-yl)benzene containing a carbodiimide moiety as a 2-azahexatriene system. The employed six-step sequence afforded trigonoine B (1) in 9.2% overall yield. The described route could be employed for the preparation of various N-substituted 4-aminopyrroloquinolines with various biological activities.


Introduction
In 2011, two novel alkaloids, namely trigonoine A and B, were isolated from the leaves of Trigonostemon lii by Hao and co-workers [1]. The structures of the compounds were elucidated through 1D and 2D NMR spectroscopy. It was determined that trigonoine A was a β-carboline alkaloid containing a 2,8diazabicyclo[3.3.1]nonane ring system, while trigonoine B (1) was formed by a combination of 2,3-dihydroquinolin-4-one and 3H-pyrrolo [2,3-c]quinoline rearranged from a β-carboline skeleton ( Figure 1).
Additionally, the antihepatitis B virus (HBV) activity of the alkaloids was evaluated in vitro using an HBV-transfected HepG2 cell line. The antihuman immunodeficiency virus (HIV) properties were also investigated to determine whether trigonoine A and B could prevent the cytopathic effects of HIV-1 IIIB in C8166 cells. Notably, it was found that both natural products exhibited anti-HIV activity.
In addition, we recently reported the total syntheses of marinoquinolines A (3a), B (3b), and E (3e) comprising the pyrrolo[2,3-c]quinoline skeleton [25]. As demonstrated in Scheme 1, Curtius rearrangement of carboxylic acid 4 resulted in the formation of isocyanate 5, which, upon electrocyclization furnished pyrrolo[2,3-c]quinoline 6. Intermediate 6 was subsequently transformed into triflate 7, and the total syntheses of marinoquinolines 3a, 3b, and 3e were accomplished by introducing different substituents at the C4 position. However, despite our efforts to introduce dihydroquinoline derivatives into triflate 7 using various conditions, the synthesis of 8 could not be achieved. Consequently, we decided to develop a new synthetic strategy for the preparation of trigonoine B (1). Scheme 1: Total synthesis of marinoquinolines and the failure of the introduction of a tetrahydroquinoline moiety by direct amination to triflate 7.
In this work, we report the first total synthesis of trigonoine B (1) involving the construction of a pyrrolo[2,3-c]quinoline framework by electrocyclization of 2-(pyrrol-3-yl)benzene containing a carbodiimide moiety as a 2-azahexatriene system.

Results and Discussion
Scheme 2 illustrates the retrosynthetic strategy designed to synthesize triogonoine B (1). It was speculated that the dihydroquinoline moiety of trigonoine B (1) could be constructed through a cycloamination reaction between positions C1a and N1. The synthesis of the precursor pyrroloquinoline 9 possessing a substituted amino group at the 4-position could be achieved by the electrocyclization of pyrrol-3-ylbenzene 10 containing a carbodiimide moiety as a 2-azahexatriene system. Lastly, it was proposed that the carbodiimide 10 could be derived from urea 11. Therefore, we investigated the electrocyclization of a pyrrol-3ylbenzene containing a carbodiimide moiety. First, 2-(pyrrol-3yl)aniline 14 was synthesized by a Suzuki-Miyaura coupling reaction of 2-iodoaniline (12) and 3-(4,4,5,5-tetramethyl-1,3,2dioxaborolan-2-yl)-1-[tris(1-methylethyl)silyl]-1H-pyrrole (13) according to Pratt's conditions (Scheme 3) [29]. Subsequently, to remove the triisopropylsilyl (TIPS) protecting group, compound 14 was treated with tetra-n-butylammonium fluoride (TBAF) in THF, affording aniline 15 in 65% yield. Treatment of 15 with phenyl isocyanate in CH 2 Cl 2 gave urea 16a in 54% yield. To obtain carbodiimide 17a, 16a was treated with carbon tetrabromide (CBr 4 ), PPh 3 , and Et 3 N in CH 2 Cl 2 . The reaction was monitored by TLC, which confirmed the complete consumption of the starting material. However, after the workup, extraction, and removal of solvent (in vacuo), the appearance of the TLC plate changed due to the formation of various byproducts. Then, the reaction mixture was purified, but the desired carbodiimide 17a was not obtained, but amino-pyrroloquinoline 18 formed through electrocyclization of 17a in 25% yield. Notably, it was found that the electrocyclization of 17a proceeded easily at low temperature (≈60 °C).  Although we tried to optimize the reaction conditions to improve the yield of 18, the yield could not be improved owing to the generation of numerous byproducts in the reaction of 16a with CBr 4 , PPh 3 , and Et 3 N. Using the same procedure, carbodiimide 17b was then synthesized in 58% yield starting from aniline 14 via urea 16b. Then, the electrocyclization of 17b was attempted, but the cyclization did not proceed at all. As possible reason we considered a steric hindrance of the TIPS group. Based on the above results, it was speculated that the electrocyclization of 17b could proceed continuously following the removal of the TIPS group. Indeed, when 17b was heated with TBAF in 1,2dichlorobenzene (1,2-DCB) at 80 °C, the expected reaction proceeded and the desired pyrroloquinoline 18 was obtained in 58% yield.
The focus subsequently shifted to the total synthesis of trigonoine B (1) (Scheme 5). The key starting material, 2-iodo-5-methoxyaniline (24), was synthesized according to the procedure previously reported by Wetzel and co-workers [31]. The Suzuki-Miyaura coupling of 2-iodoaniline derivative 24 and pyrrole-3-boronic acid pinacol ester 13 was carried out in the presence of Pd(OAc) 2 and SPhos, followed by the treatment of the resulting 2-(pyrrol-3-yl)aniline 25 with 3-(2-bromophenyl)propyl isocyanate (26a), which afforded urea 27a in 60% yield. The treatment of urea 27a with CBr 4 and PPh 3 in the presence of Et 3 N then gave carbodiimide 28a in a good yield of 74%. Following the reaction of 28a with TBAF in 1,2-DCB and desilylation, the electrocyclization of 29a proceeded smoothly to afford the desired 4-aminopyrroloquinoline 30a in 68% yield. Subsequently, the cycloamination of 30a in the presence of Pd(OAc) 2 , Cu(OAc) 2 , and K 2 CO 3 gave tetrahydroquinoline 31 in 25% yield. However, although attempts were made to optimize the cycloamination reaction conditions, the yield could not be improved. We hypothesized that the low yield could be attributed to a too low reactivity of the bromo group. Thus, the same reaction was performed using a compound bearing a more reactive iodo group.
Finally, the oxidation of tetrahydroquinoline 31 was examined. Following the evaluation of various reaction conditions [32][33][34], the best outcome was obtained upon treatment of 31 with KMnO 4 and MgSO 4 in an acetone-H 2 O solvent system [35]. Employing these conditions, trigonoine B (1) was obtained in 43% yield. The acquired physical and spectroscopic data of the herein synthesized compound 1 were consistent with those of the natural trigonoine B [1]. Thus, in this study, we successfully achieved the first total synthesis of trigonoine B (1).

Conclusion
The total synthesis of a pyrrolo[2,3-c]quinoline alkaloid, trigonoine B (1), was achieved for the first time through the electrocyclization of 2-(pyrrol-3-yl)benzene bearing a carbodiimide moiety as a 2-azahexatriene system. The employed sixstep sequence afforded the desired product 1 in 9.2% overall yield. Notably, the developed synthetic route could be used for the synthesis of various N-substituted 4-aminopyrroloquinolines. The investigation of the biological activity of trigonoine B and its derivatives is under evaluation.

Supporting Information
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